19858-14-1

Basic information

• Product Name: (methoxymethyl)thiirane
• Synonyms: (methoxymethyl)thiirane;2-(Methoxymethyl)thiirane;2,3-Epithiopropyl methyl ether;Ether, 2,3-epithiopropyl methyl;Nsc82312;Thiirane, (methoxymethyl)-;Thiirane, 2-(methoxymethyl)-
• CAS NO: 19858-14-1
• Molecular Formula: C₄H₈OS
• Molecular Weight: 104.17072
• EINECS: 243-381-0
• Mol File: 19858-14-1.mol
• Article Data: 4

Chemical Properties

• Boiling Point: 153.95°C (estimate)
• Flash Point: 28.9°C
• Appearance: /
• Density: 1.059 (estimate)
• Vapor Pressure: 15.5mmHg at 25°C
• Refractive Index: 1.5920 (estimate)
• CAS DataBase Reference: (methoxymethyl)thiirane(CAS DataBase Reference)
• NIST Chemistry Reference: (methoxymethyl)thiirane(19858-14-1)
• EPA Substance Registry System: (methoxymethyl)thiirane(19858-14-1)

Safety Data

• Hazardous Substances Data: 19858-14-1(Hazardous Substances Data)

Usage

General Description

(Methoxymethyl)thiirane is a chemical compound with the molecular formula C4H8OS. It is a heterocyclic organic compound that contains a thiirane ring with a methoxymethyl substituent. Thiiranes are three-membered cyclic sulfides containing one sulfur and two carbon atoms. (Methoxymethyl)thiirane is often used as a reagent in organic synthesis and can be involved in various chemical reactions, such as nucleophilic ring opening and addition reactions. The compound's properties and reactivity make it a useful intermediate in the synthesis of pharmaceuticals and other organic compounds.

InChI:InChI=1/C4H8OS/c1-5-2-4-3-6-4/h4H,2-3H2,1H3

Upstream product

• 930-37-0 glycidyl methyl ether 
• 57346-02-8 methoxyoxirane 
• 333-20-0 potassium thioacyanate 

Downstream Products

• 126-68-1 O,O,O-triethyl phosphorothioate 
• 627-40-7 methylallylether 
• 1746-13-0 allyl phenyl ether 
• 94953-16-9 6-phenoxy-6-methoxymethyl-4-thia-1-hexene 
• 94953-11-4 6-phenoxy-5-methylmethoxy-4-thia-1-hexene 
• 121568-08-9 MeOCH₂CH(SH)CH₂NH(m-MePh) 

Relevant articles and documents

MASS-SPECTROMETRIC CHARACTERISTICS OF GLYCIDYL AND THIOGLYCIDYL ETHERS

The principles of the fragmentation of the simplest glycidyl and thioglycidyl ethers under the influence of electron impact, which were discovered by comparison of the spectra of homologs using data from photoelectronic spectroscopy and optical mass spectrometry, are examined as a manifestation of the general characteristics of the fragmentation of bifunctional compounds.

Electronic Structure and Geometric Structure of Three-member Heterocycles. I. Photo-electron Spectra of Glycidyl and Thioglycidyl Ethers

The electronic structure of a series of glycidyl and thioglycidyl ethers has been studied by photo-electron spectroscopy.The first bands in these spectra have been identified, and correlation diagrams giving the dependence of the ionisation potential of the orbital on the nature of the substituent have been constructed.